在 COF 系列催化剂上通过电化学硝酸盐和二氧化碳合成尿素的理论研究

IF 2.1 4区 化学 Q3 CHEMISTRY, PHYSICAL Catalysis Surveys from Asia Pub Date : 2023-10-31 DOI:10.1007/s10563-023-09408-9
Yingjun Hou, Ling Guo
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引用次数: 0

摘要

催化合成尿素是哈伯-博什法和工业尿素合成法的一种有效替代方法。二氧化碳和氮氧化物在环境条件下的电化学 C-N 偶联是一种新开发的方法,它也为解决硝酸盐污染问题提供了新的思路。共轭有机框架(COFs)因其规整的结构和多孔特性,可实现高效的电子转移,已被用作氮还原反应和二氧化碳还原反应(CO2RR)的前瞻性电催化剂。本文报道了在 MoM1S-Pc-M2PPs COF(M 为过渡金属)电催化剂上以二氧化碳和硝酸盐为原料高效合成尿素的过程。根据 DFT 计算发现,二氧化碳和氧化氮很难共吸附在 MoM1S-Pc 上合成尿素,因此我们选择在金属卟啉(M2PPs)结构单元上合成 CO,然后在双金属酞菁和氧化氮上溢流合成尿素。通过计算验证了硝酸盐在不同催化剂上吸附的可能性。我们对 MoM1S-Pc 候选催化剂的稳定性、硝酸盐吸附强度和催化活性进行了筛选,结果表明最有前途的候选催化剂是 MoFeS-Pc。同时,我们还对 CO2RR M2PPs 衬底进行了筛选,并选出了最佳的 VPPs 结构。在不同含氮中间体与*CO的耦合研究中,C-N耦合机理表明*NOH和*CO是两种可能的C-N耦合含氮中间体,它们在热力学上是自发的,具有较低的活化势垒。这项研究不仅为环境条件下氮氧化物与二氧化碳偶联合成尿素提供了新的认识,而且为促进碳氮偶联产物的可持续生产铺平了道路。
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Theoretical Study on the Synthesis of Urea by Electrochemical Nitrate and Carbon Dioxide over COF Series Catalysts

Catalytic synthesis of urea is a bright substitutable to Haber–Bosch progression and industrial urea synthesis. Electrochemical C–N coupling of carbon dioxide and nitrogen oxides under environmental conditions is a newly developed method, which also provides a novel opinion for solving nitrate contamination. Conjugated organic frameworks (COFs) have been used as prospective electrocatalysts for nitrogen reduction reactions and carbon dioxide reduction reactions (CO2RR) as a result of their regulate structure and multihole properties, resulting in efficient electron transfer. This paper reports the efficient synthesis of urea from carbon dioxide and nitrate over MoM1S-Pc-M2PPs COF (M as a transition metal) electrocatalyst. According to the calculation of DFT, it was found that it was difficult for carbon dioxide and nitrogen oxide to coadsorb on MoM1S-Pc to synthesize urea, so we chose to synthesize CO on the metal porphyrin (M2PPs) structural unit, and then overflow on the bimetallic phthalocyanine and nitrogen oxide to synthesize urea. The possibility of nitrate adsorption on different catalysts was verified by calculation. We screened the stability, nitrate adsorption strength, and catalytic activity of MoM1S-Pc candidates, and the results showed that the most promising candidate catalyst was MoFeS-Pc. At the same time, the CO2RR M2PPs substrate was also screened, and the VPPs structure was selected as the best. In the study of coupling between different nitrogen-containing intermediates and *CO, the C–N coupling mechanism shows that *NOH and *CO are two possible C–N coupling nitrogen intermediates, which are shown to be thermodynamically spontaneous and have an inferior activation barrier. This study not only provisions novel perceptions into urea synthesis by coupling nitrogen oxides with carbon dioxide under environmental conditions, but also paves the way for boosting the sustainable production of carbon and nitrogen-coupled products.

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来源期刊
Catalysis Surveys from Asia
Catalysis Surveys from Asia 化学-物理化学
CiteScore
4.80
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Early dissemination of important findings from Asia which may lead to new concepts in catalyst design is the main aim of this journal. Rapid, invited, short reviews and perspectives from academia and industry will constitute the major part of Catalysis Surveys from Asia . Surveys of recent progress and activities in catalytic science and technology and related areas in Asia will be covered regularly as well. We would appreciate critical comments from colleagues throughout the world about articles in Catalysis Surveys from Asia . If requested and thought appropriate, the comments will be included in the journal. We will be very happy if this journal stimulates global communication between scientists and engineers in the world of catalysis.
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